Evidence map›Paper›PMID 26892775›Full record

ArticleScientific reports2016

A block mixture model to map eQTLs for gene clustering and networking.

Ningtao Wang, Kirk Gosik, Runze Li, Bruce Lindsay, Rongling Wu

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ningtao WangDepartment of Biostatistics, University of Texas School of Public Health, Houston, TX 77030, USA.
Kirk GosikDepartment of Statistics, The Pennsylvania State University, University Park, PA 16802, USA.
Runze LiDepartment of Biostatistics, University of Texas School of Public Health, Houston, TX 77030, USA.
Bruce LindsayDepartment of Biostatistics, University of Texas School of Public Health, Houston, TX 77030, USA.
Rongling WuDepartment of Biostatistics, University of Texas School of Public Health, Houston, TX 77030, USA.

Funding

Constitutive and Agent-Based Multiscale Models to Improve Vein Graft SurvivalU01HL119178 · NHLBI · UNIVERSITY OF FLORIDA · PI BERCELI, SCOTT A, GARBEY, MARC · 2013 to 2018
$2.7M
NHLBI NIH HHS U01 HL119178NHLBI NIH HHS UO1 HL119178
6 · The paper itself

Abstract

To study how genes function in a cellular and physiological process, a general procedure is to classify gene expression profiles into categories based on their similarity and reconstruct a regulatory network for functional elements. However, this procedure has not been implemented with the genetic mechanisms that underlie the organization of gene clusters and networks, despite much effort made to map expression quantitative trait loci (eQTLs) that affect the expression of individual genes. Here we address this issue by developing a computational approach that integrates gene clustering and network reconstruction with genetic mapping into a unifying framework. The approach can not only identify specific eQTLs that control how genes are clustered and organized toward biological functions, but also enable the investigation of the biological mechanisms that individual eQTLs perturb in a signaling pathway. We applied the new approach to characterize the effects of eQTLs on the structure and organization of gene clusters in Caenorhabditis elegans. This study provides the first characterization, to our knowledge, of the effects of genetic variants on the regulatory network of gene expression. The approach developed can also facilitate the genetic dissection of other dynamic processes, including development, physiology and disease progression in any organisms.

Indexed as

Chromosome MappingGene Regulatory NetworksMultigene FamilyQuantitative Trait LociAnimalsCaenorhabditis elegansCluster AnalysisComputational BiologyGenome-Wide Association StudyGenotypeReproducibility of ResultsROC Curve

Identifiers

PMID26892775
PMCPMC4759821

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.